Canonical Allele Identifier: PA2827963198
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2809Pro
CA16039553
NM_001354897.2:c.8425T>C